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Targeting Endocytosis  and Cell Communications  in the Tumor Immune Microenvironment

The existence of multiple endocytic pathways is well known, and their exact biological effects in tumors have been intensively investigated. Endocytosis can affect the connection between tumor cells and determine the fate of tumor cells. Many relationships between endocytosis and tumor cells have be...

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Autores principales: Wu, Bo, Wang, Qian, Shi, Xiang, Jiang, Meixi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578241/
https://www.ncbi.nlm.nih.gov/pubmed/36258231
http://dx.doi.org/10.1186/s12964-022-00968-3
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author Wu, Bo
Wang, Qian
Shi, Xiang
Jiang, Meixi
author_facet Wu, Bo
Wang, Qian
Shi, Xiang
Jiang, Meixi
author_sort Wu, Bo
collection PubMed
description The existence of multiple endocytic pathways is well known, and their exact biological effects in tumors have been intensively investigated. Endocytosis can affect the connection between tumor cells and determine the fate of tumor cells. Many relationships between endocytosis and tumor cells have been elucidated, but the mechanism of endocytosis between different types of cells in tumors needs to be explored in greater depth. Endocytic receptors sense the environment and are induced by specific ligands to trigger communication between tumor and immune cells. Crosstalk in the tumor microenvironment can occur through direct contact between cell adhesion molecules or indirectly through exosomes. So a better understanding of the endocytic pathways that control cell adhesion molecules and function is expected to lead to new candidates for cancer treatment. In additional, tumor-derived exosomes may changes immune cell function, which may be a key role for tumors to evade immune detection and response. The overall understanding of exosomes through endocytosis is also expected to bring new candidates for therapeutic regulation of tumor immune microenvironment. In this case, endocytic pathways coordinate cell adhesion molecules and exosomes and can be used as targets in the tumor immune microenvironment for cancer treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-022-00968-3.
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spelling pubmed-95782412022-10-19 Targeting Endocytosis  and Cell Communications  in the Tumor Immune Microenvironment Wu, Bo Wang, Qian Shi, Xiang Jiang, Meixi Cell Commun Signal Review The existence of multiple endocytic pathways is well known, and their exact biological effects in tumors have been intensively investigated. Endocytosis can affect the connection between tumor cells and determine the fate of tumor cells. Many relationships between endocytosis and tumor cells have been elucidated, but the mechanism of endocytosis between different types of cells in tumors needs to be explored in greater depth. Endocytic receptors sense the environment and are induced by specific ligands to trigger communication between tumor and immune cells. Crosstalk in the tumor microenvironment can occur through direct contact between cell adhesion molecules or indirectly through exosomes. So a better understanding of the endocytic pathways that control cell adhesion molecules and function is expected to lead to new candidates for cancer treatment. In additional, tumor-derived exosomes may changes immune cell function, which may be a key role for tumors to evade immune detection and response. The overall understanding of exosomes through endocytosis is also expected to bring new candidates for therapeutic regulation of tumor immune microenvironment. In this case, endocytic pathways coordinate cell adhesion molecules and exosomes and can be used as targets in the tumor immune microenvironment for cancer treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-022-00968-3. BioMed Central 2022-10-18 /pmc/articles/PMC9578241/ /pubmed/36258231 http://dx.doi.org/10.1186/s12964-022-00968-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Wu, Bo
Wang, Qian
Shi, Xiang
Jiang, Meixi
Targeting Endocytosis  and Cell Communications  in the Tumor Immune Microenvironment
title Targeting Endocytosis  and Cell Communications  in the Tumor Immune Microenvironment
title_full Targeting Endocytosis  and Cell Communications  in the Tumor Immune Microenvironment
title_fullStr Targeting Endocytosis  and Cell Communications  in the Tumor Immune Microenvironment
title_full_unstemmed Targeting Endocytosis  and Cell Communications  in the Tumor Immune Microenvironment
title_short Targeting Endocytosis  and Cell Communications  in the Tumor Immune Microenvironment
title_sort targeting endocytosis  and cell communications  in the tumor immune microenvironment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578241/
https://www.ncbi.nlm.nih.gov/pubmed/36258231
http://dx.doi.org/10.1186/s12964-022-00968-3
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